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Associate Scientist


DPS Group Global is currently seeking for an Associate Scientist who is responsible for conducting research in assigned areas under direct supervision using established methodology.

Years of Experience Req.:
>2 years
Date Posted:
Days Remaining:
Employment Type:
Education Level Req.:
Bsc or Msc degree


DPS is a leading Project Management and Engineering Company serving industry around the world for 40 years. Our reputation is based on forming successful partnerships with our clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.
We provide Full Service Engineering for our clients including Project and Programme Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification and Start-up on numerous projects across a range of market sectors. Our Main market sectors are; Pharmaceutical and Biotechnology, Medical Technologies, Oil & Gas, Advanced Technology, Science & Education, Food & Beverage, and Energy.



  • Taking part in activities related to the production of cGMP batches. This includes processes such as batch record review and taking escalations from cell and virus culture, purification processes, formulation & fill and in-process testing.
  • Accurately completion of documentation such as batch records, logbooks, etc.
  • Working precisely, detecting and solving acute problems and communicate possible abnormalities.
  • Actively participating in setting up documentation to ensure successful production runs.
  • Responsible as area owner that the production areas are according EHSS and compliance standards.
  • Internal organiz776231.910019ation of the facility, including ISL, 5S and kanban systems.
  • Involvement in deviation investigation and follow up.
  • Write training documentation and perform training of new operators.


Skills & Education

  • Bachelor or Master level or equivalent
  • 2-6 years’ experience in a biotechnology or biopharmaceutical industry environment.
  • GMP experience, either in the pharma or medical device sector
  • English and speaking, writing, and verbal skills are fluent (Dutch is a plus but not required)
  • Able to set priorities
  • Quality, efficiency, accuracy and reliability of work
  • Planning, adherence to timelines
  • Innovating capabilities
  • Communication capabilities
  • Quality of SOP's
  • Personal targets


Additional Details

Full time preferred, 32 hours discussable. Options to extend beyond current end date are not immediately evident, but in case of strong performance and continued workload, there may be a possibility to continue. This person's job would be to support production from "the outside", eg on documentation review and update, handling escalations. This job does not involve hands-on execution, however they will be visiting production and support the operators. We could be flexible to consider a young ambitious engineer, as well as more senior options.


Available and interested?

please send your resume to: [email protected] or give us a call +31(0)715730810

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